setting up the perfusion chamber to measure contractility in isolated, pressurized lymph vessels

Analisi in tempo reale del calcio e della contrattilità nei vasi linfatici isolati

The lymphatic vasculature is found in many organ systems including the brain, heart, lungs, kidney, and mesentery1,2,3,4,5,6, and operates by propelling fluid (lymph) from the interstitial spaces to the central venous ducts to maintain fluid homeostasis7,8,9,10. It starts with blind-ended lymphatic capillaries within the vascular capillary beds that drain into collecting lymph vessels (LVs). Collecting LVs are made of two layers of cells: a layer of endothelial cells encompassed by a layer of lymphatic muscle cells (LMCs)10,11. Lymph fluid transport is achieved through both extrinsic forces (e.g. new lymph formation, arterial pulsations, central venous pressure fluctuations) and intrinsic forces12.
The intrinsic force for lymph transport is the spontaneous rhythmic contraction of collecting LVs, which is the focus of the majority of studies investigating lymphatic function. This intrinsic lymphatic pump is principally regulated by the cyclic rise and fall of cytosolic, free Ca2+ ([Ca2+]i). Spontaneous depolarization of the plasma membrane in LMCs activates voltage-gated &#34;L-type&#34; Ca2+ (Cav1.x) channels triggering Ca2+ influx and subsequent LV rhythmic contraction8,9,10. This role was demonstrated by blocking Cav1.x with specific agents, like nifedipine, which inhibited LV contractions and caused vessel dilation13,14. The transient rise in [Ca2+]i or &#34;Ca2+ spike&#34; in the LMCs mediated by Cav1.x channels also may mobilize intracellular Ca2+ stores by activating inositol triphosphate (IP3) receptors and ryanodine receptors (RyRs) on the sarcoplasmic reticulum (SR)15,16,17,18. Current evidence suggests IP3 receptors contribute more Ca2+ required for normal LV contractions compared to RyRs15,16,19,20,21; however, RyRs may play a role during pathology or in response to pharmaceutical intervention17,18. Additionally, the activation of Ca2+-activated K+ channels22 and ATP-sensitive potassium (KATP) channels23,24 can hyperpolarize the LMC membrane and inhibit spontaneous contractile activity.
There are many other ion channels and proteins that may regulate Ca2+ dynamics in collecting LVs. Utilizing methods to study changes in Ca2+ and vessel contractility in response to pharmacological agents in real time is important to understand these potential regulators. An earlier method using Fura-2 to measure relative changes in LV [Ca2+]i has been described25. Because the dissociation constant for Fura-2 and Ca2+ is known26, it is possible to calculate actual concentrations of Ca2+, which broadens the application of this method and provides additional insight into Ca2+ signaling, membrane excitability, and contractility mechanisms27, as well as allowing for baseline comparisons between experimental groups. This latter approach has been used in cardiomyocytes28, and therefore, can be adapted to LVs. This paper presents an improved method that combines these two approaches to measure and calculate changes in absolute [Ca2+]i as well as vessel contractility/rhythmicity continuously in real time in isolated, pressurized LVs. We also provide representative results for LVs treated with nifedipine.

Autore in primo piano: Metodi innovativi nella ricerca sul linfedema e l'ipertensione

Valutazione in tempo reale del Ca2+ assoluto, citosolico, libero e della corrispondente contrattilità in vasi linfatici isolati e pressurizzati

Impostazione della camera di perfusione per misurare la contrattilità nei vasi linfatici isolati e pressurizzati

Per iniziare, prendi le micropipette in vetro borosilicato acquistate da una fonte commerciale. Tagliare e lucidare le micropipette a una lunghezza di circa uno o due centimetri per l'uso nella camera di perfusione del vaso isolato. Collegare ogni cannula di vetro montata nella camera di perfusione del recipiente a trasduttori di pressione indipendenti allineati con regolatori di pressione indipendenti alimentati a gravità e collegati tramite tubi in polietilene.Riempire la camera di profusione, le micropipette di vetro e il regolatore di pressione alimentato a gravità insieme al tubo in polietilene con la soluzione salina fisiologica, quindi bloccare la pressione per assicurarsi che le cannule non siano pressurizzate.

setting-up-perfusion-chamber-to-measure-contractility-isolated

Research

JoVE Journal

Immunology and Infection

Setting Up the Perfusion Chamber to Measure Contractility in Isolated, Pressurized Lymph Vessels

211 Views. Per iniziare, prendi le micropipette in vetro borosilicato acquistate da una fonte commerciale. Tagliare e lucidare le micropipette a una lunghezza di circa uno o due centimetri per l'uso nella camera di perfusione del vaso isolato. Collegare ogni cannula di vetro montata nella camera di perfusione del recipiente a trasduttori di pressione indipendenti allineati con regolatori di pressione indipendenti alimentati a gravità e collegati tramite tubi in polietilene.Riempire la camera di ...

Video: Impostazione della camera di perfusione per misurare la contrattilità nei vasi linfatici isolati e pressurizzati

Real-time Evaluation of Absolute, Cytosolic, Free Ca2+ and Corresponding Contractility in Isolated, Pressurized Lymph Vessels

The lymphatic vasculature, now often referred to as &#34;the third circulation,&#34; is located in many vital organ systems. A principal mechanical function of the lymphatic vasculature is to return fluid from extracellular spaces back to the central venous ducts. Lymph transport is mediated by spontaneous rhythmic contractions of lymph vessels (LVs). LV contractions are largely regulated by the cyclic rise and fall of cytosolic, free calcium ([Ca2+]i).
This paper presents a method to concurrently calculate changes in absolute concentrations of [Ca2+]i and vessel contractility/rhythmicity in real time in isolated, pressurized LVs. Using isolated rat mesenteric LVs, we studied changes in [Ca2+]i and contractility/rhythmicity in response to drug addition. Isolated LVs were loaded with the ratiometric Ca2+-sensing indicator Fura-2AM, and video microscopy coupled with edge-detection software was used to capture [Ca2+]i&#160;and diameter measurements continuously in real time.
The Fura-2AM signal from each LV was calibrated to the minimum and maximum signal for each vessel and used to calculate absolute [Ca2+]i. Diameter measurements were used to calculate contractile parameters (amplitude, end diastolic diameter, end systolic diameter, calculated flow) and rhythmicity (frequency, contraction time, relaxation time) and correlated with absolute [Ca2+]i measurements.

This protocol describes a method to simultaneously measure cytosolic, free calcium [Ca2+]i and vessel diameter in contracting lymph vessels in real time and then calculate absolute Ca2+ concentrations as well as contractility/rhythmicity parameters. This protocol can be used to study Ca2+ and contractile dynamics across a variety of experimental conditions.

The lymphatic vasculature, now often referred to as &#34;the third circulation,&#34; is located in many vital organ systems. A principal mechanical ...

Ricerca

Immunologia e infezioni

Isolation and Cannulation of Mesenteric Lymph Vessels to Measure Cytosolic, Free Calcium and Vessel Diameter in Contracting Lymph Vessels

Isolamento e incannulamento dei vasi linfatici mesenterici per misurare il calcio citosolico, libero e il diametro dei vasi nei vasi linfatici in contrazione

Methods Article

Impostazione della camera di perfusione per misurare la contrattilità nei vasi linfatici isolati e pressurizzati